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Prevalence of rhinosinusitis among atypical cystic fibrosis patients

European archives of oto-rhino-laryngology, 2011-04, Vol.268 (4), p.519-524

2011

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Association of a nonsense mutation (W1282X), the most common mutation in the Ashkenazi Jewish cystic fibrosis patients in Israel, with presentation of severe disease

American journal of human genetics, 1992-01, Vol.50 (1), p.222-228

1992

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Mild cystic fibrosis and normal or borderline sweat test in patients with the 3849 + 10 kb C-->T mutation

The Lancet (British edition), 1993-07, Vol.342 (8862), p.25-26

1993

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A New Mutation in the CFTR Gene, Composed of Two Adjacent DNA Alterations, Is a Common Cause of Cystic Fibrosis among Georgian Jews

Genomics (San Diego, Calif.), 1993, Vol.15 (1), p.236-237

1993

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Serum Endothelin-1, MMP-9, and Myeloperoxidase and Coronary Artery Morphology as Detected by Multi-Slice CT Angiography in Intermediate and High Risk Asymptomatic Subjects

The open biomarkers journal, 2010-02, Vol.3 (1), p.7-12

2010

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Mild cystic fibrosis and normal or borderline sweat test in patients with the 3849 + 10 kb C → T mutation

The Lancet (British edition), 1993-07, Vol.342 (8862), p.25-26

1993

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642 TIMP-4 SINGLE NUCLEOTIDE POLYMORPHISM AND CARDIAC FUNCTION IN HEART FAILURE PATIENTS

Atherosclerosis. Supplements, 2011-06, Vol.12 (1), p.135-135

2011

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P45 ASSOCIATION OF ET-1, MMP-9, AND MYELOPEROXIDASE WITH CORONARY MORPHOLOGY DETECTED BY CT ANGIOGRAPHY IN MODERATE–HIGH RISK ASYMPTOMATIC SUBJECTS

Atherosclerosis. Supplements, 2010-06, Vol.11 (2), p.26-26

2010

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Pulmonary Alveolar Proteinosis in a Hypogammaglobulinemic Infant

Pediatric asthma, allergy & immunology, 1998, Vol.12 (2), p.151-156

1998

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Mild cystic fibrosis and normal or borderline sweat test in patients with the 3849 + 10 kb→T mutation

The Lancet (British edition), 1993, Vol.342 (8862), p.25-26

1993

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Association of a nonsense mutation (W1282X), the most common mutation in the Ashkenazi Jewish cystic fibrosis patients in Israel, with presentiation of severe disease

American journal of human genetics, 1992, Vol.50 (1), p.222-228

1992

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Effectiveness of PTC124 treatment of cystic fibrosis caused by nonsense mutations: a prospective phase II trial

The Lancet (British edition), 2008-08, Vol.372 (9640), p.719-727

2008

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Beyond the mouse model: Using Drosophila as a model for sperm interaction with the female reproductive tract

Theriogenology, 2010-04, Vol.73 (6), p.723-739

2010

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p53 is required for brown adipogenic differentiation and has a protective role against diet-induced obesity

Cell death and differentiation, 2013-05, Vol.20 (5), p.774-783

2013

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Chronic ataluren (PTC124) treatment of nonsense mutation cystic fibrosis

The European respiratory journal, 2011-07, Vol.38 (1), p.59-69

2011

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p53 Counteracts reprogramming by inhibiting mesenchymal-to-epithelial transition

Cell death and differentiation, 2013-02, Vol.20 (2), p.312-320

2013

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Multicenter cross-sectional study of nontuberculous mycobacterial infections among cystic fibrosis patients, Israel

Emerging infectious diseases, 2008-03, Vol.14 (3), p.378-384

2008

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Gentamicin-Induced Correction of CFTR Function in Patients with Cystic Fibrosis and CFTR Stop Mutations

The New England journal of medicine, 2003-10, Vol.349 (15), p.1433-1441

2003

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The clinical significance of micronutrients in relation to immune functions

Annals of the New York Academy of Sciences, 1990, Vol.587 (1), p.55-58

Rivlin, R.S. (Memorial Sloan-Kettering Cancer Center, New York, NY)

1990

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Placing search in context: the concept revisited

ACM transactions on information systems, 2002-01, Vol.20 (1), p.116-131

2002

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Magnesium deficiency and alcohol intake: mechanisms, clinical significance and possible relation to cancer development (A review)

Journal of the American College of Nutrition, 1994-10, Vol.13 (5), p.416-423

Rivlin, R.S. (Memorial Sloan-Kettering Cancer Center, NY, NY.)

1994

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Local Shuffling of Spike Trains Boosts the Accuracy of Spike Train Spectral Analysis

Journal of neurophysiology, 2006-05, Vol.95 (5), p.3245-3256

2006

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The onset of p53 loss of heterozygosity is differentially induced in various stem cell types and may involve the loss of either allele

Cell death and differentiation, 2014-09, Vol.21 (9), p.1419-1431

2014

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Nitrite dynamics in the open ocean—clues from seasonal and diurnal variations

Marine ecology. Progress series (Halstenbek), 2012-05, Vol.453, p.11-26

2012

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Managing acute pain with inhaled methoxyflurane in non-cancer patients: a review of the latest evidence

Current opinion in supportive & palliative care, 2024-09

2024

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Prevalence of rhinosinusitis among atypical cystic fibrosis patients

Association of a nonsense mutation (W1282X), the most common mutation in the Ashkenazi Jewish cystic fibrosis patients in Israel, with presentation of severe disease

Mild cystic fibrosis and normal or borderline sweat test in patients with the 3849 + 10 kb C-->T mutation

A New Mutation in the CFTR Gene, Composed of Two Adjacent DNA Alterations, Is a Common Cause of Cystic Fibrosis among Georgian Jews

Serum Endothelin-1, MMP-9, and Myeloperoxidase and Coronary Artery Morphology as Detected by Multi-Slice CT Angiography in Intermediate and High Risk Asymptomatic Subjects

Mild cystic fibrosis and normal or borderline sweat test in patients with the 3849 + 10 kb C → T mutation

642 TIMP-4 SINGLE NUCLEOTIDE POLYMORPHISM AND CARDIAC FUNCTION IN HEART FAILURE PATIENTS

P45 ASSOCIATION OF ET-1, MMP-9, AND MYELOPEROXIDASE WITH CORONARY MORPHOLOGY DETECTED BY CT ANGIOGRAPHY IN MODERATE–HIGH RISK ASYMPTOMATIC SUBJECTS

Pulmonary Alveolar Proteinosis in a Hypogammaglobulinemic Infant

Mild cystic fibrosis and normal or borderline sweat test in patients with the 3849 + 10 kb→T mutation

Association of a nonsense mutation (W1282X), the most common mutation in the Ashkenazi Jewish cystic fibrosis patients in Israel, with presentiation of severe disease

Effectiveness of PTC124 treatment of cystic fibrosis caused by nonsense mutations: a prospective phase II trial

Beyond the mouse model: Using Drosophila as a model for sperm interaction with the female reproductive tract

p53 is required for brown adipogenic differentiation and has a protective role against diet-induced obesity

Chronic ataluren (PTC124) treatment of nonsense mutation cystic fibrosis

p53 Counteracts reprogramming by inhibiting mesenchymal-to-epithelial transition

Multicenter cross-sectional study of nontuberculous mycobacterial infections among cystic fibrosis patients, Israel

Gentamicin-Induced Correction of CFTR Function in Patients with Cystic Fibrosis and CFTR Stop Mutations

The clinical significance of micronutrients in relation to immune functions

Placing search in context: the concept revisited

Magnesium deficiency and alcohol intake: mechanisms, clinical significance and possible relation to cancer development (A review)

Local Shuffling of Spike Trains Boosts the Accuracy of Spike Train Spectral Analysis

The onset of p53 loss of heterozygosity is differentially induced in various stem cell types and may involve the loss of either allele

Nitrite dynamics in the open ocean—clues from seasonal and diurnal variations

Managing acute pain with inhaled methoxyflurane in non-cancer patients: a review of the latest evidence

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